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. 2012 Oct 4;7(2):370–383. doi: 10.1038/ismej.2012.109

Table 1. Primers used in this study for cDNA clone library construction and real-time PCR quantification of arsenic biotransformation-related genes (arrA and arsB/acr3) and the housekeeping gene recA.

Target Primer set Forward primer (5'–3') Reverse primer (5'–3') Annealing temperature (°C) Amplicon size (bp) Reference or source
arrA Clone library HAArrA-D1F/HAArr-G2R CCGCTACTACACCGAGGGCWWYTGGGRNTA CGTGCGGTCCTTGAGCTCNWDRTTCCACC 53.5 ∼500 Kulp et al., 2006
  Real-time PCR qArr1F/qARR1R GATCCACGCTTCTCCACCTC CCCCGGCTTTAAAGAGGTTC 60 ∼172 This study
arsB Clone library AarsB1F/AarsB1R GAACATCGTCTGGAAYGCNAC GTACACCACCAGRTACATNCC 55 ∼750 Achour et al., 2007a
acr3-1 Clone library Aacr1F/Aacr2R GGCCTGATCGTNATGATGTAYCC GCGATGGCCAGCTCRAARTTRTT 57b ∼750 Achour et al., 2007a
  Real-time PCR qA1-3F/qA1-2R ATGGCCAGCTCGAAaTTGTT   60 ∼94 This study
acr3-2 Clone library dacr5F/dacr4R TGATCTGGGTCATGATCTTCCCVATGMTGVT CGGCCACGGCCAGYTCRAARAARTT 52 ∼750 Achour et al., 2007a
  Real-time PCR qA2-1F/qA2-1R GGCCAGTTCGAAGAAGTTGG GCCGATTTTGATCCAGGTGT 60 ∼127 This study
recA Clone library recA-48F/recA-583R CCAGATHGARAARCAGTT TTCATACGGATCTGGTTGAT 55 ∼540 This study
  Real-time PCR qrecA-2F/qrecA-3R TTGAGAAGCAGTTCGGCAAA CGGTCCGAAGATCTCGATG 60 ∼156 This study
a

Primers modified by Fahy et al., unpublished.

b

57°–0.5° for 10 cycles, 52° for 30 cycles.